Persistent URL of this record https://hdl.handle.net/1887/3564811
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Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial disease
- All authors
- Lee, R.G.; Balasubramaniam, S.; Stentenbach, M.; Kralj, T.; McCubbin, T.; Padman, B.; Smith, J.; Riley, L.G.; Priyadarshi, A.; Peng, L.Y.; Nuske, M.R.; Webster, R.; Peacock, K.; Roberts, P.; Stark, Z.; Lemire, G.; Ito, Y.A.; Boycott, K.M.; Geraghty, M.T.; Klinken, J.B.; Ferdinandusse, S.; Zhou, Y.; Walsh, R.; Marcellin, E.; Thorburn, D.R.; Rosciolli, T.; Fletcher, J.; Rackham, O.; Vaz, F.M.; Reid, G.E.; Filipovska, A.; Care4Rare Canada Consortium
- Date
- 2022-02-11
- Journal
- Human Molecular Genetics
- Volume
- 31
- Issue
- 21
- Pages
- 3597 - 3612